Population Genomic Screening in Primary Care - Pre-Application Webinar
Attend a 59-minute webinar hosted by the National Human Genome Research Institute on September 10, 2024, focusing on the pre-application process for Population Genomic Screening in Primary Care Notices of Funding Opportunities (NOFOs). Learn about the im…
I Have a Family Member with Dementia - Am I at Risk?
Explore genetic factors in dementia, understand testing options, and learn about the rarity of hereditary causes in this informative presentation by a genetic counselor.
NextGen Genomic Medicine - Making Variants of Unknown Significance Obsolete
Explore cutting-edge genomic medicine and its impact on understanding genetic variants. Learn how advanced techniques are revolutionizing the interpretation of previously unknown genetic variations in cardiovascular health.
Pharmacogenomics: Personalizing Medication Through Genetic Testing
Explore pharmacogenomics testing: its potential for personalizing medication and current limitations in clinical application.
Genes, Family Trees, and Complex Disease
Explore genetics, family history, and disease risk. Learn about genetic testing and environmental factors in complex diseases.
Clinical Interpretation of Genes and Variants for Disease Causality - MPG Primer 2022
Dive into clinical interpretation of genes and variants for disease causality with expert Heidi Rehm. Explore standardized approaches, open science, and data sharing in genomic medicine and rare disease gene discovery.
Deep Learning-Based Morphological Profiling for Rare Disease Genomic Medicine
Explore deep learning-based morphological profiling for rare disease genomics. Uncover innovative approaches to overcome batch effects and improve out-of-distribution generalization in fluorescent microscopy data analysis.
The Real World Phenotypic Presentation of Mendelian Disease - CGSI 2024
Explore the complex real-world phenotypic manifestations of Mendelian diseases through Lisa Bastarache's insightful presentation at CGSI 2024, delving into recent research and clinical implications.
Establishing and Sustaining Genomic Learning Healthcare Systems
Experts discuss progress and challenges in implementing genomic medicine, focusing on evidence generation, payer perspectives, and integration of personalized medicine in healthcare systems.
Genomic Sequencing and the Medicine Revolution
Explore the genomic medicine revolution and its impact on healthcare through advancements in sequencing technology and personalized treatments.
Ambry Genetics - Applications of Diagnostic Exome Sequencing
Explore diagnostic exome sequencing applications in neonatal intensive care, covering methods, results, case studies, and benefits of early genetic diagnosis for newborns.
Genomic Medicine and Microbial Research - 2021 AAAS Annual Meeting President's Address
Pioneering genomic scientist Claire Fraser discusses her groundbreaking work in microbial genomics and its impact on medicine, including her current research on the human gut microbiota.
Genomic Medicine XV: Population Screening - Welcome and Keynotes - Session 1
Explore the current state, barriers, and opportunities of population genomic screening in the U.S., discussing its impact on clinical practice, technologies, costs, and future research directions.
Genetic Testing in Adult Neurology Patients
Explore the utility and diagnostic yield of genetic testing in adult neurology patients, reviewing recent research findings and implications for clinical practice.
Opportunistic Screening for Medically Actionable Secondary Genomic Findings
Explore communication and outcomes of medically actionable secondary genomic findings, identifying research gaps and opportunities for genetic counselors to enhance precision medicine approaches.
Community Engagement and Population Genomic Screening - Session 4
Explore community engagement strategies and ethical considerations for population genomic screening, with a focus on Indigenous populations and the All of Us Research Program.
Evidence Needed to Support Genomic Population Screening - Session 5
Experts discuss population genomic screening, covering value propositions, cost-effectiveness, implementation experiences, and specific case studies like APOL1 screening, to inform future research and clinical practice.
Logistics of Population Screening in Genomic Medicine - Session 3
Explores challenges and opportunities in population genomic screening, addressing readiness, timing, underrepresented populations, provider training, and patient education for improved healthcare outcomes.
Obstacles to Genomic Medicine and Population Screening - Session 6
Explore challenges in genomic screening: payer reluctance, data sharing complexities, EHR integration, and demonstrating health benefits. Experts discuss obstacles and potential solutions.
Genomic Medicine XV - Research Directions, Summary and Next Steps
Explore the latest developments in genomic medicine, focusing on population screening, barriers, opportunities, clinical impact, technologies, costs, and future research directions.
Genomic Medicine XV: Laying the Groundwork for Population Genomic Screening - Session 1
Explore genomic medicine's current state, barriers, and future in population screening. Experts discuss technologies, clinical impact, and research directions for expanded genomic screening in the U.S.